| autosomaal dominante hereditaire motorische en sensorische neuropathie type 2I (aandoening) | | autosomaal dominante hereditaire motorische en sensorische neuropathie type 2I | | autosomaal dominante CMT 2I
autosomaal dominante HMSN 2I
autosomaal dominante ziekte van Charcot-Marie-Tooth type 2I
| | Autosomal dominant Charcot-Marie-Tooth disease type 2I | | A form of axonal Charcot-Marie-Tooth disease a peripheral sensorimotor neuropathy. A late onset with severe sensory loss associated with distal weakness mainly of the legs and absent or reduced deep tendon reflexes. |
| | Id | 717013009 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | G60.0 | | Term | Hereditaire motorische en sensorische neuropathie |
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| SNOMED CT to Orphanet simple map | 99942 |
| SNOMED CT to ICD-10 extended map | | Target | G60.0 | | Rule | TRUE | | Advice | ALWAYS G60.0 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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